Hydrochloric Acid → HCID 21938661, compound

HRID 2087053Notes

Reaction equation

HRID 2087053 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[C:4]([F:9])[C:3]=1[N:10]([C:18](=[O:21])[CH2:19]Cl)[C:11]1[CH:16]=[CH:15][C:14]([CH3:17])=[CH:13][CH:12]=1.[Cl-].[Al+3].[Cl-].[Cl-].ClC1C=CC=CC=1Cl.Cl>O>[Cl:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[C:4]([F:9])[C:3]=1[N:10]1[C:11]2[C:16](=[CH:15][C:14]([CH3:17])=[CH:13][CH:12]=2)[CH2:19][C:18]1=[O:21]

Participants

6

Procedure

To a mixture of 100 g (0.3 mol) of N-(2′-chloro-4′,6′-difluorophenyl)-N-chloroacetyl-4-methylaniline and 103 g (0.78 mol) of aluminum chloride is added 400 ml of 1,2-dichlorobenzene. The reaction is heated to 140° for 2 hours. The reaction is cooled to room temperature and added to a mixture of 100 ml of concentrated HCl and 700 ml water (cooled to 0-5° in a dry ice/acetone bath). The mixture is extracted twice with 400 ml of methylene chloride. The combined organic layers are washed with 600 ml of 3N HCl. The organic layer is stirred with 66 g of magnesium sulfate and 33 g of charcoal (DARCO G-60). The solids are filtered off and the solvents are evaporated under reduced pressure to give a tan solid which is recrystallized from ethanol to give N-(2′-chloro-4′,6′-difluorphenyl)-5-methyloxindole, mp 137-140°.

Workup

  1. temperatureThe reaction is heated to 140° for 2 hours
  2. extractionThe mixture is extracted twice with 400 ml of methylene chloride
  3. washThe combined organic layers are washed with 600 ml of 3N HCl
  4. filtrationThe solids are filtered off
  5. customthe solvents are evaporated under reduced pressure
  6. customto give a tan solid which
  7. customis recrystallized from ethanol

Sources & evidence

ORD record
ord-395542904a7847a3905a17d60bb9f556
Source dataset
uspto-grants-2004_04
Patent number
US06727281B2

Reaction notes

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